|
HS Code |
316722 |
| Iupac Name | 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone |
| Molecular Formula | C5H6N2OS |
| Molar Mass | 142.18 g/mol |
| Cas Number | 1122-62-9 |
| Appearance | White to off-white solid |
| Melting Point | 246-250 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Smiles | CC1=CC(=O)NC(=S)N1 |
| Pubchem Cid | 76146 |
| Synonyms | 6-Methylthiouracil |
| Inchi | InChI=1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9) |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25g of 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone, tightly sealed, labeled with hazard and identification information. |
| Container Loading (20′ FCL) | 20′ FCL container loading: Product packed in 25kg fiber drums, 9 metric tons per 20′ container, securely stacked for transport. |
| Shipping | **Shipping Description:** 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone is shipped in a tightly sealed container, protected from light and moisture. It should be transported in compliance with local regulations for laboratory chemicals, labeled for research use only, and stored at room temperature upon arrival. Ensure appropriate documentation accompanies the shipment. |
| Storage | Store **6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep away from incompatible substances such as strong oxidizing agents. Use appropriate personal protective equipment when handling, and ensure proper labeling of the storage container to avoid accidental misuse or contamination. |
| Shelf Life | 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone typically has a shelf life of 2 years when stored in a cool, dry place. |
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Sifting through sacks of fine powders day after day, small details in a molecule’s makeup often prove far more crucial than they appear on a dry specification sheet. In the case of 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone, actual experience in producing and processing this compound gives us solid ground for understanding both its strengths and its quirks. Our crews see it as a workhorse among pyrimidine derivatives, often crossing paths with it in the blending rooms and during granulation. The chemical formula, C5H6N2OS, becomes more than a line in a book when you realize just how consistently it delivers results, especially in pharmaceutical intermediate synthesis and agricultural chemical research.
Years at the reactors teach us that attention to temperature and moisture levels during crystallization can shift yield and purity outcomes more than theory suggests. Batch documentation doesn’t tell the whole story. From the manufacturer’s standpoint, a purity over 99% is achievable with the right combination of time, controlled solvent addition, and seed crystal selection, a method passed down the line through hands-on training rather than just lab instruction. Production teams keep a watchful eye on fine needle-shaped crystals that come out at the right temperature window. Purity and form influence the downstream reactions of customers, especially contract pharmaceutical accounts.
This pyrimidinone’s structure—bearing both a methyl group at the 6-position and a thioxo group—guides its selectivity in synthesis. We’ve watched process chemists favor it for certain nucleophilic reactions, citing both the ease of handling and the predictive outcomes in ring modifications. Laboratories tied to generic drug research or seed treatment formulations make regular purchases directly from our site, often after troubleshooting results with our technical staff who handle the material themselves.
On the factory floor, specifications and test reports are as much daily log entries as they are customer assurances. The accepted melting point range, generally between 285°C and 290°C (decomposition), gets checked in every shift, with every lot. While analytical certificates confirm data for paperwork, hands-on verification keeps deviations low. Experienced technicians measure moisture content meticulously, flagging anything over 0.5%, which can foreshadow storage or solubility issues down the line. No laboratory instrument replaces the human eye watching for off-color tints or irregularities in crystal form—issues that can suggest contamination or solvent retention.
Our own history in manufacturing this compound goes back more than a decade, and each year brings small refinements to how we check for side products. HPLC and NMR give us detailed fingerprints, but years at the controls teach that even subtle spectral changes may point to a drift in feedstock quality or a temperature slip in the reaction kettle. This vigilance is what separates batches that pass from those that need rework, and customers in both pharma and agrochemical development have learned to ask about the year-over-year stability of these results.
Early on, process improvements centered on solvent recovery and atmospheric controls—investments made to meet both environmental and customer requirements. Today, a production run sized at 500kg uses closed-loop nitrogen blanketing and near-complete solvent reclamation, both for worker safety and cost savings. The result is fewer off-gas events and tighter control over trace impurity levels, something that end-users working on regulated applications have repeatedly favored.
There’s no substitute for careful handling practices. Transporting finished product from crystallizers to drum filling lines without exposure to high humidity or extraneous contaminants takes routine, discipline, and constant attention. Dedicated climate-controlled packaging lines have cut call-backs from customers over lumping or caking nearly to zero over the last five years. Bulk packaging consists of triple-layer bags sealed in durable drums, a method we adopted after early experience with punctured sacks and lost product back in the early 2010s.
As a powder, 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone disperses evenly in most production solutions. Mixing teams use variable-speed stirrers to reduce dust formation, a practice developed partly to protect operators and partly to avoid product loss. Solubility in water remains low, but when pre-wetted with isopropanol or acetone, blending becomes trouble-free. This habit developed out of necessity after several customer batches turned up poor dispersion profiles with dry-powder additions. We took the time to run parallel tests using both dry and moistened forms, confirming better batch consistency with the latter—a tip we regularly pass on.
End-users working on pilot-scale synthesis often ask about shelf life and stability. Our direct records, inspecting stock held at both ambient and sub-ambient warehouses, confirm the powder maintains stability and color for more than two years when kept under dry and cool conditions. We’ve observed product degradation only after long exposures to direct sunlight or moisture. Shipping teams ensure tamper-evidence and clear labeling on every drum, reducing mix-ups and supporting traceable transport throughout the supply chain.
In regular operations, the difference between this pyrimidinone and similar heterocyclic bases comes into focus. The 6-methyl substitution and thioxo group push reactivity in specific directions, supporting synthesis schemes that standard pyrimidinones simply cannot achieve. Customers who need reliable nucleophilicity and strong selectivity in ring modification reactions make this molecule a mainstay in their toolkits.
Compared to other pyrimidine-based intermediates, including 2,4-dioxo or 2-thio compounds lacking the methyl group, our teams have documented tried-and-true performance advantages in terms of both chemical yield and speed of downstream transformation. For instance, generic pharmaceutical makers report that final active ingredient quality improves when this compound is used during stage-two intermediates, especially in small-molecule antivirals and herbicide candidates. These claims aren’t just stories; five years of local and international export records back up continuing orders, often with detailed technical follow-up from returning clients.
Research teams tell us they encounter fewer side reactions and less need for repetitive purification when starting procedures use this methyl-thioxo derivative. The predictable results stem from our real production parameters—consistent moisture levels, rigorous impurity testing, and feedback-driven process improvements from both manufacturing and application labs. Researchers replacing less selective analogues with this material have reported yield increases of up to 12% in select syntheses, something documented through both customer case studies and our own pilot-plant trials.
From the very start, working directly with pyrimidine family intermediates grounds you in the importance of responsible material handling. This thioxo pyrimidinone is no exception. Standard best practices—ventilated work areas, dust-reduction methods, and sealed packaging—have all come from years of close observation and feedback from operators. Direct skin or eye contact remains a risk like with many fine powders, so every packaging line runs with safety glasses and gloves as part of the normal routine.
Storage under nitrogen or in dry rooms nearly eliminates clumping and degradation. By putting airtight drum closures in place and using humidity cards in each container, we’ve documented better preservation of original appearance and reactivity, reducing returns and complaints. Our own regulatory team tracks updates in local and international chemical management rules, and every production lot ships with detailed batch origin and quality paperwork—elements now expected by most regulated-pharmaceutical and agrochemical processors.
Looking back through company records, only minor adjustments have been needed for safety documentation over the years, a sign that process stability and thorough risk prevention have become second nature in our operation. Discussions with customers on safe handling and disposal only reinforce the shared responsibility to minimize workplace and environmental impact.
As more customers come to us for tailored quantities and particle sizes, our plant has invested in scalable reaction controls and custom blending services. Large-scale synthesis up to the tonnage level relies heavily on control of reaction exotherms and precise solvent management, while small-batch lines let us cater to specialty research projects needing just a few kilograms. The technical flexibility comes from decades of in-house engineering, not just spec sheets or equipment catalogs.
The rise of custom application requests has shifted our operating approach. We routinely prepare micronized batches for high-dispersion needs and granulated forms for bulk-processing customers. The shift from single-use drum filling to flexible, multi-use tote systems helps both our large and small clients manage their inventories and reduce waste. End-of-line inspection and mixing mean customers receive product ready to immediately charge into their own processes, skipping extra pre-processing time.
Our experience in changing between lot sizes for different clients—pharma, crop science, academic research—has underscored the need for flexibility that chemists on the ground genuinely appreciate. In one case, a research team needed a particle size reduction to boost solubility in a pilot scale; several test batches later, we delivered just that. The extensiveness of our line conversion capability comes from hands-on troubleshooting, not just written procedures.
Over the years, every improvement in yield, handling, and storage has come from direct practice, repeated trials, and constant interaction with field users. One early investment in solvent reclamation both reduced emissions and improved lot reproducibility. Our efforts with direct moisture measurement and packaging upgrades have paid off in fewer rejected lots each quarter.
We field frequent requests for product with different impurity thresholds, driven by the needs of both regulated and academic customers. A dynamic approach to production and blending allows us to address these requirements in real time, whether for extra purification or custom blending ratios. Technical support staff maintain close relationships with scientists at client labs, often collaborating to solve one-off synthesis complications or to adapt product formats for new workflows. These are not arm’s-length transactions but cooperative efforts that improve results for everyone.
Our plant continues to implement operator feedback and customer suggestions into process updates. Case in point: one pilot-lot run for a university research group led us to introduce a new packaging configuration, keeping the powder dry even through long overseas freight. A field trial with an agricultural customer showed the value of pre-moistening product to reduce on-site dust, leading us to share this best practice broadly with others using similar workflows.
Looking ahead, shifting regulations and expanding customer applications bring new technical hurdles and opportunities. The constant among all these changes remains material reliability—something rooted in years of practical manufacturing experience, daily vigilance on the production floor, and open communication between our staff and the end users shaping the future of pharmaceutical and agricultural technology.
At the core of our work stands an understanding built from years producing and shipping 6-Methyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone—not just for today’s order, but with an eye toward what longer-term partnerships really require: consistency, transparency, and technical expertise grounded in real use. Anyone who’s spent time at the drum-filling line or a blending bench knows that paper specs only matter as much as the hands and minds standing behind them. That is what makes all the difference.